Canonical Allele Identifier: CA772723488
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1482897136
gnomAD v3: 17-49363331-TTTTC-T
gnomAD v4: 17-49363331-TTTTC-T
MyVariant Identifiers: chr17:g.47440694_47440697del (hg19) chr17:g.49363332_49363335del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363335_49363338del , CM000679.2:g.49363335_49363338del GRCh38
NC_000017.10:g.47440697_47440700del , CM000679.1:g.47440697_47440700del GRCh37
NC_000017.9:g.44795696_44795699del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110882.1:n.136+818_136+821del
NR_110883.1:n.31-944_31-941del
NR_110884.1:n.58-944_58-941del
Search 100 bp 5'
Search 100 bp 3'